Anterior cervical instrumentation systems, methods and devices

ABSTRACT

Anterior cervical instrumentation systems, methods, and devices are disclosed. Systems may facilitate immobilizing or providing support for the cervical portion of the vertebral column of a patient. A device may comprise a plate having two channels located in a proximal to distal direction, and may further comprise at least one aperture. The device may further comprise attachment elements such as attachment cross-links and spacer cross-links, and fasteners. The plate and the attachment elements may be secured to the vertebrae by passing fasteners through apertures and channels. The length of the plate, position and number of the attachment cross-links, position and number of spacer cross-links and degree of movement may be intraoperatively selected by the surgeon to provide an optimal application and procedural outcome. Uniform components of the devices and systems allow for a more streamlined and simplified method of treating spinal conditions.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part claiming priority under 35 U.S.C. §120 to U.S. patent application Ser. No. 12/554,220, entitled “ANTERIOR CERVICAL INSTRUMENTATION SYSTEMS, METHODS AND DEVICES,” filed 4 Sep. 2009, which claims priority under 35 U.S.C. §119(e) to U.S. Provisional Patent Application Ser. No. 61/094,340 filed 4 Sep. 2008, which is hereby incorporated in its entirety as if fully set forth herein.

TECHNICAL FIELD OF THE INVENTION

Embodiments of the present invention relate to implantable surgical stabilization systems, devices, and methods for use in spinal surgery, and particularly to systems, methods, and devices that stabilize the cervical spine or other osseous structures.

BACKGROUND OF THE INVENTION

Fusion of spinal vertebrae is often necessary to relieve debilitating pain or to correct a deformity. Cervical spinal fusion is often prescribed for patients suffering from degenerative disk disease whose symptoms may include neck pain of discogenic origin with degeneration of the disk confirmed by patient history and radiographic studies, trauma including fractures, tumors, deformity such as kyphosis, lordosis or scoliosis, pseudoarthrosis, or failed previous fusions.

Spinal surgical fusion is the process of bringing together two or more vertebrae under conditions whereby the vertebrae fuse together to form a unitary member of the spinal column. When vertebrae are fused, e.g., with bone grafts, graft extenders, or interbody spacers such as interbody cages or boxes (collectively termed “grafts” herein), it is desirable to stabilize the fused vertebrae using an apparatus such as a plate to fixate one cervical vertebra to another to promote fusion across motion segments. In carrying out the procedure, the members must be brought together under conditions that are critically controlled to prevent infection, maintain alignment of opposing members, and allow for the stress in the bone that is generated as the healing process matures. Immobilization is an important requirement during this healing process.

Another common spinal ailment is the degeneration of an intervertebral disc caused by trauma, disease, and/or aging. A degenerated intervertebral disc may have to be partially or fully removed from a spinal column. Partial or full removal of an intervertebral disc may destabilize a spinal column. Destabilization of a spinal column may alter the natural separation distance between adjacent vertebrae. Maintaining a natural separation distance between vertebrae may help prevent pressure from being applied to nerves that pass between vertebral bodies. Excessive pressure applied to the nerves may cause pain and/or nerve damage. During a spinal fixation procedure, a spinal implant may be inserted in a space created by removal or partial removal of an intervertebral disc between adjacent vertebrae. A spinal implant may maintain the height of the spine and restore stability to the spine. Intervertebral bone growth may fuse the implant to adjacent vertebrae.

A spinal implant may be inserted during a spinal fixation procedure using an anterior, lateral, or posterior spinal approach. A discectomy may be performed to remove or partially remove a defective and/or damaged intervertebral disc. A discectomy creates a disc space for a spinal implant. After a discectomy, a spinal implant may be inserted into the disc space. One or more spinal implants may be inserted between a pair of vertebrae. Spinal implants may be inserted into disc spaces prepared between more than one pair of vertebrae during a spinal fusion procedure.

A spinal plate may be coupled to vertebrae after insertion of one or more spinal implants. A spinal plate may stabilize the vertebrae and inhibit back out of the spinal implant from between vertebrae. A spinal plate may share a compressive load applied to one or, more spinal implants inserted between vertebrae. Fasteners, such as bone screws, may couple the spinal plate to vertebrae. Spinal plates may stabilize sections of cervical spine and/or sections of lumbar, spine.

The process of bone healing has been widely studied. Micro-fractures, once thought to be negative events, are now seen as part of the natural process of bone remodeling and occur within bone in the course of everyday wear and tear. In the early stage of these cycles, bone resorption is first accomplished by osteoclasts. This is followed by new bone formation by osteoblasts over the latter part of each cycle. Osteoblasts serve a critical role in new bone formation, filling in the bony cavity in areas of bone remodeling with bone matrix. Osteoblasts are further known to release cytokines to attract osteoclasts. Osteoclasts serve to release proteases, which act to dissolve bone mineral matrix, collagen, and clear away damaged bone. Osetoclasts also releases matrix-bound growth factors and may serve as a chemo attractant for osteoblasts. The process of bone healing is currently believed to be a continual cycle, in which the body's response to microfractures and stress injuries within healing bone actually serve to strengthen healing ultimately and produce more solid bone.

What is needed are systems, methods and devices such as a plating system to repair bone fractures or to stabilize separate bony structures and allow them to fuse into a single item that may incorporate or harness the elements of the natural bone healing process. What are needed are systems, methods and devices that promote optimal fusion at a graft, particularly at cervical vertebrae. Further, methods, systems and devices that utilize a minimum number of parts and which may be easily customized intraoperatively by the surgeon are also needed.

BRIEF SUMMARY OF THE INVENTION

The present invention is directed to spinal instrumentation systems, methods and devices. The present invention comprises plating systems for use in spinal treatments, including, but not limited to, the cervical spine. Embodiments of the present invention are directed to anterior cervical instrumentation systems. Such systems may facilitate immobilizing or providing support for the cervical portion of the vertebral column of a patient. Such systems are composed of plates and screws for aligning and holding vertebrae in a desired position relative to one another. The systems may be “stand alone” as instrumentation is applied only to the anterior portion of the vertebral column (cervical vertebrae), or the systems may include other devices or compositions such as instrumentation on the posterior vertebral column. The systems, methods and devices allow a surgeon to modify and customize system components intraoperatively for optimal fit.

The present invention comprises systems, methods and devices comprising an implantable device for affixing to the anterior side of vertebrae, such as cervical vertebrae, for stabilizing the spinal column. Systems and devices of the present invention comprise a plate having an anterior surface and a posterior surface. A plate may comprise two parallel elongate channels extending from the distal end of the plate to the proximal end of the plate. Each of the channels forms an elongated opening through plate. A plate may further comprise at least one aperture, which may be centrally located, or at least one aperture at both the distal and proximal ends, and for stability reasons, may comprise two apertures at both the distal and proximal ends. The apertures may function in attaching the plate to a spinal vertebra using fasteners, such as screws. For example, apertures may be round, oval or rounded rectangular or combinations of these or others in shape. The systems may comprise a plurality of different length plates, which allows a surgeon the flexibility to select the desired length plate pre- or intraoperatively.

Systems and devices of the present invention may further comprise attachment elements for attaching the plate to one or more spinal vertebrae or for stabilizing the plate device. For example, a system and device may comprise a plurality of elements referred to herein as cross-linking elements. Cross-linking elements comprise at least two types of elements which may be similar in design, but differ in function. The two types of cross-linking elements comprise attachment cross-links and spacer cross-links and, for example, each may be a small bar that is as long as the plate is wide, with a defined width, that has two apertures, and each aperture may have the diameter of the apertures of the plate, and may also be sized so that a fastener, such as a screw, is sized to pass through the cross-linking aperture and also pass through the channel. Cross-linking element apertures may be located near both ends of a cross-linking element so that the apertures of the cross-linking elements align with each of the two channel openings in a plate.

The attachment elements comprise fasteners, elements for directly attaching the plate or attachment cross-links to the vertebrae, or attaching spacer cross-links to the plate, and such fasteners may comprise pins, dual head pins or screws. Fasteners may be sized to pass through the apertures of the cross-linking elements, the channels, and the apertures of the plates. Fasteners comprise a pin having two heads, wherein each head is spaced apart so that each pin head may enter a plate channel or two adjacent apertures.

Methods of the present invention comprise methods of spinal treatment, including treatment of the cervical spine. Methods comprise approaching the cervical spine from an anterior position. Using a template of a plate of the present invention, the exact location and placement of a plating system and device on the patient is determined. The template may be used on the exposed vertebrae or on x-rays or other visualizations of the spinal area. The size of plate to be used, the number cross-linking elements and attachment sites, where the attachment elements are to be placed through the plate apertures and the cross-link apertures is determined. Thus, the size of the plate and cross-link placement may individualized for the patient during the surgical procedure.

The appropriately sized plate may then be placed over the anterior portion of the vertebrae and anchored in place by the placement of fasteners, such as screws, through the at least one aperture, such as those found on the proximal and distal ends of the plate. The plate may be held in place with a temporary fastener, including but not limited to, a dual-headed pin. The pin is temporary in that the pin is placed through the plate to temporarily anchor the plate to the bone(s), for example to examine placement of the plate and alignment of the pin, and then the pin is removed. The pin may serve as a guide for bone screws which anchor the plate in place.

The proximal and distal apertures of a plate can be of several types. The first type may have the apertures of the same size and be round in shape, which allows for semi-constrained movement at the screw heads. Another type may have proximal and distal apertures that would be slightly elongated in the vertical axis, referred to herein as oval, to allow for translational movement at the proximal and distal ends of the plate. Another type may have proximal and distal apertures that would be elongated in the vertical axis, referred to herein as rounded rectangular, to allow for translational movement at the proximal and distal ends of the plate.

One or more attachment cross-links may be placed on the anterior side of the plate in the predetermined locations for attachment of the plate to the vertebrae, and attached to the vertebrae. For example, the plate and attachment cross-link may be attached to a spinal vertebra by passing a screw through each of the apertures of the cross-link and the parallel channels of the plate, and into the bone. The attachment cross-link may be fixed in position relative to the bone, but may move relative to the plate as the screws move in the parallel channels of the plate. Alternatively, the attachment cross-links may be spring loaded to lock it in position relative to the plate. The attachment cross-link may be positioned relative to the plate at any point along the length of the channels. Consequently, the surgeon may custom fit the location of the attachment cross-link to the bone because the position is not limited by predetermined screw holes in the plate.

Once one or more attachment cross-links are coupled to the vertebral bones, spacer cross-links may be fastened to the plate. The spacer cross-links do not attach to vertebrae, but fill the channel space on the device where the attachment cross-links are not present and function to stabilize the device. The entire length of the channels of the plate that are not occupied by the attachment cross-links may be filled with the spacer cross-links until there remains little or no open space in the channels of the plate. The spacer cross-links may be attached to the plate using a variety of fasteners, including, but not limited to, a hole-to-hole clamp or a screw head, or a short screw. The distance between the cross-links may be determined by the surgeon to create a range of travel of the attachment cross-link to provide a desired degree of subsidence. In this manner, the attachment cross-link attached to the bone may be locked in place relative to the plate or may have a predetermined degree of movement. The fasteners for attaching the plate device to the bone, such as screws, may be maintained in place by using locking heads or other designs known in the art.

An aspect of the present invention comprises systems, methods and devices wherein the plates may be provided in multiple lengths, but the apertures of the plates and the cross-linking elements, and the channel sized openings are uniform and allow for the use of the same size and style fastener head, such as the same screw head, for attachment of cross-linking elements, though the lengths of the fasteners may be a variety of lengths. This allows the surgeon to use one instrument, such as the same screw driver implement, to attach the plate to the vertebrae and to stabilize the device. The size, such as length and width of the cross-linking elements, is uniform and may be used with any length plate. This uniformity allows for a more simplified system for the surgeon to use, and for fewer tools to be needed in the operating theater.

These and other features as well as advantages, which characterize various aspects of the present invention, will be apparent from a reading of the following detailed description and a review of the drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A illustrates an exemplary embodiment of a plate of the present invention.

FIG. 1B illustrates an exemplary embodiment of a plate of the present invention.

FIG. 1C illustrates an exemplary embodiment of a plate of the present invention.

FIG. 1D illustrates a side view an exemplary embodiment of a plate attached to a region of the spinal column.

FIG. 2 illustrates an exemplary embodiment of a system having a plurality of plates.

FIG. 3A illustrates three embodiments of cross-linking elements.

FIG. 3B illustrates an embodiment of a dual-headed pin.

FIG. 3C illustrates an embodiment of an offset dual-headed pin.

FIG. 3D illustrates an embodiment of placement of an offset dual-headed pin.

FIGS. 4A and B illustrate a top view of a plate and cross-linking elements of an exemplary embodiment of the present invention.

FIG. 5 illustrates a side view of an exemplary embodiment of the system attached to a spinal column.

FIG. 6A illustrates the Globus interbody spacer.

FIG. 6B illustrates a cross-sectional view of an implanted Globus interbody spacer.

FIG. 6C illustrates the Synthes interbody spacer.

FIG. 6D illustrates a cross-sectional view of an implanted Synthes interbody spacer.

FIGS. 7A and 7B illustrate two embodiments of an adapting cross-linking element.

FIGS. 8A and 8B illustrate two embodiments of coupling elements.

FIGS. 9A and 9B illustrate cross-section views of an adapting cross-linking element attached to an interbody spacer with two embodiments of coupling elements.

FIG. 10A illustrates a cross-sectional view of a plate coupled to three interbody spacers.

FIG. 10B illustrates a cross-sectional view of a plate coupled to two non-adjacent interbody spacers with a skipped level between.

FIG. 10C illustrates a cross-sectional view of a plate coupled to two interbody spacers where the interbody spacers are not sequential and a standard ACDF cage is located between the two interbody spacers.

FIG. 11 illustrates a front view of a plate with coupled to connection to three interbody spacers.

FIG. 12A illustrates a cross-sectional views of a plate used to reinforce an interbody spacers.

FIG. 12B illustrates a cross-sectional view of a plate used in a salvage procedure to reinforce an interbody spacers where it was necessary for the screws in the interbody spacer to be removed.

FIG. 13 illustrates a cross-sectional view of a plate used to reinforce an interbody spacer.

DETAILED DESCRIPTION OF THE INVENTION

The present invention comprises methods, systems and devices for treatment of spinal vertebrae, such as cervical vertebrae. The present invention comprises implantable devices comprising plates and attachment elements that allow for aligning and maintaining adjacent vertebrae, including but not limited to, cervical vertebrae, in a selected spatial relationship. The present invention may be used in spinal fusion methods.

The present invention comprises anterior cervical plating systems and devices that allow for the intersegmental compression of the spinal segment, such as compression of the adjacent vertebrae and the fusion graft in the disc space between the adjacent vertebrae, in lordosis, and where desired, multisegmental compression. For example, a device of the present invention comprises a plate, attachment elements comprising cross-linking elements comprising attachment cross-links and spacer cross-links, and fasteners, elements for directly attaching the plate and cross-linking elements to the bone, or attaching cross-linking elements to the plate, including, but not limited to, screws and dual-headed pins. For example, a system of the present invention comprises a plurality of plates of various lengths, and uniformly sized attachment elements and fasteners with uniform head design, and having multiple lengths. The invention further comprises tools and instruments used with such systems and devices in methods of spinal treatment such as drills, taps, screw drivers and the like.

Systems and devices of the present invention comprise a plate, which may be provided in a length that is sufficient to span a disc space and to overlap, at least in part, at least two adjacent cervical vertebrae. The anterior and posterior surfaces of a plate may be the same or may be different, in that one of the surfaces, such as the posterior surface which faces the vertebrae, may be textured and/or treated to induce bone growth or aid in attachment or stability. The plate, and other elements of the systems and devices, may be made of the same or different materials, such as steel, titanium, plastics, ceramics, or other biocompatible materials that have the structural strength and durability to withstand the cyclical loading associated with long term fixation. Materials that are also compatible with visualization systems, such as fluoroscopy or MRI, are also contemplated by the present invention. The plate and other elements may also comprise bioresorbable materials, bone in-growth materials, and/or growth promoting materials. For example, such bioresorbable, bone in-growth, or bone growth promoting materials may be found on surfaces of the plate and/or attachment elements such as screws. A plate of the present invention may be curved transverse to the longitudinal axis to conform to the anterior surface of a vertebrae, or may be curved along the longitudinal axis to conform to the lordotic curvature between the vertebrae, or may not be curved at all, or may be made of a material so that a surgeon or other personnel may curve the plate at the time of surgery, or may be made of a material that does not allow curving by a surgeon or other personnel.

A plate of the present invention comprises an anterior surface and a posterior surface and the two surfaces may be the same or different over the whole surface or a part of the surface areas. For example, the posterior surface, which directly faces the vertebrae surface, may be textured or coated with a material so as to encourage bone growth. For example, the anterior surface may be textured so as to allow better purchase of the attachment elements. The plate comprises a distal end and a proximal end. An aperture may be found on one or both of the distal or proximal ends, or may be located in a central position at the distal or proximal ends, or between the channels at one or both of the proximal or distal end areas, or in a midline position.

An example of a plate of the present invention comprises at least one aperture on both the proximal and the distal ends, and may further comprise at least two apertures on at least one of the proximal or distal ends, or at least two apertures on both the proximal and distal ends. The apertures may be the same size diameter or may have differently sized diameters. An example of the present invention comprises a plate having at least two apertures at both the proximal and distal ends that are of the same size diameter. An example of the present invention comprises a plate have at least one aperture at the midline of the plate equidistant between the channels. An example of the present invention comprises a plate having one or more apertures with the same size diameter or differently sized diameters. An example of the present invention comprises a plate having one or more apertures on the at least the proximal or distal end(s) where the apertures are longer in vertical length than the screw head to allow for true translational movement at both ends.

Where the one or more apertures on the distal and proximal ends of the plate are round or where the aperture allows for little adjustment for screw placement, the movement of the plate is based upon semi-constrained movement at the screw heads. Where the one or more apertures on the distal and proximal ends of the plate are elongated so that the vertical length is longer than the horizontal length, as in oval or rounded rectangular shaped apertures, there may be movement of the embedded screws in relation to the plate to allow for translational movement. Where the one or more apertures on the distal end are different from the one or more apertures on the proximal end, for example wherein rounded apertures are present on the proximal end to provide semi-constrained movement and one or more elongated or oval apertures are found at the distal end, translational movement is provided. Similarly, apertures in the cross-linking elements also allow for semi-constrained or translational movement depending on the shape of the aperture. The movement may be constrained by use of apertures having a particular shape that locks a screw tightly with the aperture. For example, the screw head and the aperture shape may be complementary so that a tight junction is formed between the screw head and the top of the aperture. For example, the aperture may be shaped like a star or other figure into which the screw head or a locking head fits exactly and constrains the movement at that location.

A plate of the present invention comprises at least two channels that are open from the anterior to the posterior surfaces, and which form openings that traverse a substantial portion of the length of the plate. The at least two channels run from an area near an aperture found at the distal end to an area near an aperture found at the proximal end, or where there are no apertures on the ends of the plate, the channels run from near the proximal end to near the distal end. The width of a channel may be the same or different size as the diameter of an aperture of a plate. An example of the present invention comprises a plate having two channels having widths of the channel openings that are the same as the diameter of the apertures of the plate, wherein the apertures of the plate have the same sized diameter.

Devices and systems of the present invention comprise attachment elements. Attachments elements comprise cross-linking elements and fasteners, elements that interact intimately with the bone or that attach cross-linking elements to a plate, such as screws and dual-headed pins. Cross-linking elements comprise attachment cross-links and spacer cross-links. Cross-linking elements are rectangular shaped bars that fit transversely across a plate, and for example, may be as long as a plate is wide. Cross-linking elements may have no apertures or at least one aperture. For example, a cross-linking element has two apertures that are located so that an aperture is on each end of the cross-linking element, so that when the cross-linking element is placed on the anterior surface of a plate, the cross-linking apertures align with the two channels of the plate. The apertures of a cross-linking element may have the same or different diameter as that of the plate aperture(s), and/or may have the same or different diameter as that of the width of the plate channels. An example of the present invention comprises a device having apertures of the same diameter, and having channel widths that are the same as the aperture diameters of the plate and the cross-linking elements. An example of the present invention comprises a device having apertures of the same diameter, and having channel widths that are the same as the aperture diameters or widths of the cross-linking elements.

An attachment cross-link is used for attaching the device to a bone, such as a vertebra. The attachment cross-link may have as many apertures as the plate has channels, for example, an attachment cross-link has two apertures that will align with two channels of a plate. An attachment cross-link is placed transversely across the anterior surface of a plate and an aperture of the attachment cross-link provides an opening though the cross-linking element and on through the channel opening of the plate. An attachment cross-link length may be shorter or longer than the width of the plate. An attachment cross-link may be as thick as or thinner than the thickness of the plate. An attachment cross-link may be textured on either its anterior or posterior surface, for example, so that texturing on its posterior surface meshes with texturing on the anterior surface of the plate, or either or both surfaces of the attachment cross-link may have a material that promotes bone in growth, bone growth, or aids in healing soft tissues. It is contemplated by the present invention that in use, an attachment cross-link is held with the device by the passing of a fastener such as a screw or pin through each of the aperture(s) of the attachment cross-link, through the channel opening of the plate and into the bone of the vertebrae. The head of the screw would engage with the attachment cross-link and the other end of the screw would be secured in the bone, and lock the attachment cross-link to the plate and the device to the bone.

A spacer cross-link is used for stabilizing the device. A spacer cross-link is placed transversely across the plate in the area of the channels where the attachment cross-link(s) is not present. In use, the spacer cross-links occupy the area between the proximal and distal ends of the plate where the channels are and provide stability to the device. A spacer cross-link may have as many apertures as the plate has channels, for example, a spacer cross-link has two apertures that will align with two channels of a plate. A spacer cross-link is placed transversely across the anterior surface of a plate and the two apertures of the spacer cross-link provide an opening though the cross-linking element and on through the channel opening of the plate. A spacer cross-link may be shorter or longer than the width of the plate. A spacer cross-link may be as thick as or thinner than the thickness of the plate. A spacer cross-link may be textured on either its anterior or posterior surface, for example, so that texturing on its posterior surface meshes with texturing on the anterior surface of the plate, or either or both surfaces of the spacer cross-link may have a material that promotes bone in growth, bone growth, or aids in healing soft tissues. It is contemplated by the present invention that in use, a spacer cross-link is held with the device by the passing of a fastener such as a short screw through each of the aperture(s) of the spacer cross-link, or by use of a spring loaded mechanism that clamps the spacer element to the plate, or by other methods of attachment. For example, the head of a short screw would engage with the anterior surface of the spacer cross-link and the other end of the screw may be flush with the posterior surface of the plate, which would lock the spacer cross-link to the plate.

A spacer cross-link may or may not be the same size, as in length, width, and/or thickness, as the attachment cross-link. For example, a system and device of the present invention comprise attachment cross-links and spacer cross-links that are the same length, width and thickness, and have the same number and size apertures. Such a system and device would comprise only one type of cross-linking element that could be used for attachment and for spacing purposes. Such a system would use a fastener such as a screw, having only one diameter head, which may be provided in longer and shorter lengths, depending on the use of the cross-linking element, long for attachment and shorter for spacing. This would provide for use of only one type of screw driver. Such a system and device provides for uniform components to be used in implanting the device, and simplifies the methods and decisions performed by the surgeon.

Attachment elements of the present invention comprise fasteners, elements that interact intimately with the bone, or that attach cross-linking elements to a plate, such as bone screws, screws, bolts, pins, dual-headed pins, rivets, projecting elements, cements, plastics, or other components that may attach the plate to the bone or cross-linking elements to a plate. A description is provided herein comprising screws, but the invention is not necessarily limited to the use of only screws for this purpose. An aspect of the present invention provides for a device that allows for the placement of screws entering bone have sufficient angular freedom relative to the plate, in the variability of the axis of screw placement in the superior, inferior, medial and lateral directions. In the present invention, the surgeon may insert the bone screws into the vertebrae as to best to fit the anatomy of the individual patient, or multi-axial placement of a screw, such as at any angle up to 10-20 degrees from normal to the surface of the plate. The bone screws may be of a length that is sufficient for unicortical or bicortical placement. The bone screws may be self tapping, or may be inserted after tapping or drilling procedures, or after pin placement and removal. The bone screws may be locked into place with locking mechanisms known to those skilled in the art, such as a locking cap, locking ring, or a threaded cap. The screws used in the present invention for bone attachment may all be identical or different. For example, the screws used in the present invention are identical in length, width, and head design. For example, the screws used with attachment cross-links are identical to screws used with spacer cross-links in width and head design, but not in length.

Methods of the present invention comprise use of the systems and devices disclosed herein for treatment of spinal disease, damage or other conditions and pathologies. For example, a common approach for the surgical management of cervical disk disease is anterior cervical spinal fusion. The procedure for cervical spinal fusion is initiated by incising a small opening in the front of the neck. There is minimal trauma to the neck tissues. The damaged disk and/or bone spurs may be removed anterior to the spinal cord. This approach allows for minimal spinal or cord traction. Frequently, if there is significant spinal cord compression or if there is more than one disk level involved, a small plate is affixed on the anterior surface of the cervical vertebrae to provide greater permanent stability.

In a method of the present invention for anterior cervical spinal fusion, the following steps are performed. A template of a plate of the present invention may be used to determine placement of the plate, the attachment cross-links, the number of spacer cross-links needed, and the placement and angular location of the screws. A template is a replica of a plate of a particular length, and may be of a material that allows for visualization of the area under the template, i.e., may be transparent, and may be capable of having measurements written on it. The template may be used once the spinal vertebrae are exposed or may be used with x-rays or other visualization data. While the device components are being assembled based on the determinations made from the template placement, operating personnel may be preparing the vertebrae for insertion of screws, such as by pre drilling sites or tapping. Alternatively, no template is used and alternatively sized plates are used to make the determinations of placement and components.

A method of the present invention comprises temporary attachment of the plate to the vertebral bones. A plate may be held in place on the anterior spine temporarily by the use of pins, including, but not limited to, dual headed pins. The plate may be held in position using an instrument that allows for the insertion of temporary pins in apertures found at both the distal and proximal ends of a plate, or in the proximal and distal ends of elongated channels in plates that do not have end apertures. An inserter allows for a dual-head pin to be placed through the aperture or channel with visualization techniques, such as fluoroscopy. Use of the dual-headed pin and visualization allows the surgeon to determine the correct angle of placement for the screws that will follow the pins, to determine the correct length of the screws, and whether the plate is centrally and correctly aligned along the long axis of the vertebral bodies.

The dual-headed pins as disclosed herein are a single construct with an inserter that causes the pin heads to be placed in a parallel relationship. The placement of the pins under fluoroscopy aids in correct alignment in the sagittal and coronal planes. If the plate is correctly aligned coronally (not tilted to one side vertically), with lateral imaging, the dual pins will appear as one pin. If there is no or poor coronal alignment, two pins will show. If the pins are aligned coronally, but are not equally placed in the vertebral bodies, then under lateral visualization, the pins will be parallel, but one pin will appear to be deeper than the other pin.

The dual-headed pin, or any other pin known in the art, are contemplated to be of a sufficient size such that the placement in the bone and removal creates a tract or path for the bone screw or other fastener to follow. A pin or dual-headed pin may be disposable, in that it may be used only once, or may be reusable as long as the pin is structurally sound.

As an example, the surgeon can align the plate first and then select the best angle to place the pins under direct fluoroscopy. Pins, such as the dual-headed pin, may have pin heads of several lengths, ranging from about 8 to about 28 mm, from about 10 to about 25 mm, from about 12 to about 20 mm, from about 12 to about 16 mm, from about 15 to about 20 mm. Use of the pins allows for the estimation of the length of the bone screws to be used. The nonparallel angles of entry may prevent exact measurement of the length needed by the screws, but the present invention provides for a close approximation of the longest screws that can be safely used to attach the plate.

When elongated apertures are used, a dual-headed pin would be located in the upper portion of the upper (proximal) apertures, and the lower portion of the lower (distal) apertures, which would allow for translational dynamic movement once the device is assembled on vertebral bodies with screws or other attachment elements in place. For convenience, proximal and distal are in relation to the head, with items closer to the head being proximal.

To allow for true translational movement, the dual headed pin could have a 1-2 mm off-set on one side. This off-set would allow for pin placement in the upper end of the plate to have the off-set turned down and for pin placement in the lower end of the plate to have the off-set turned superior. The pins will fit into the upper portion of the upper (proximal) apertures and the lower portion of the lower (distal) apertures insuring the correct placement to allow translational dynamic movement. See FIG. 3C for a side view of a dual head pin with an offset, wherein the pin heads are offset from the central plane of the dual head pin. The b indicates the side of the pin with the offset, as does the ribbing on the handle 355, to indicate in which direction the pin heads are offset. See FIG. 3D for an example of placement of two dual headed pins with offset pin heads. In FIG. 3D, only one distal and proximal apertures are shown with pin placement and direction of the pin, indicated by a and b, are shown. The body of the pin is not shown. In practice, the dual headed pin with offset pin heads would be placed in the apertures, or in elongated channels, with the pins in the upper portion of the proximal apertures or channels and in the bottom of the lower (distal) apertures. The pin could be a single device that is flipped over for placement in either the upper or the lower apertures. The dual head pin could be labeled or color-coded to indicate the off set side. For example, FIG. 3C shows ribbing 355 on the side of the pin head offset for easy identification by a user.

In an embodiment where there are no end apertures and the at least two channels are elongated from the proximal area to the distal area, an aperture may be present in a central midline position between the channels. This central aperture may be used to provide minimal fixation of the plate without significant bone disruption during the initial placement of the plate for sizing. Once a pin is in place in the central aperture, differently sized plates could be placed on the pin to ascertain the correctly sized plate for that patient. Once the plate is selected, temporary dual-headed pins could be used to anchor the plate distally and proximally by putting in a pin at each end of the channels. The cross-linking elements and attachment elements such as bone screws can then be used to completely anchor the device to the vertebral bodies. The pins may be removed when the screws which replaced them are to be provided. Translational movement is possible with a plate having elongated channels without end apertures.

Once a compatible plate and attachment elements are determined, the plate may be attached to the selected vertebrae by providing temporary pin placements or by providing screws through the plate apertures to affix the plate at least at one end. The plate may be affixed to at least two vertebrae by providing screws through the distal and proximal end apertures, or by providing other attachment elements. The screws may follow a tract made by the placement and removal of a temporary pin, or one of the heads of a dual-headed pin. One or more attachment cross-links are added to the plate by providing temporary pins followed by screws or screws only or other fasteners only, through the attachment cross-link, through the channels of the plate and into the vertebral bone. Spacer cross-links are added to the plate, around the attachment cross-links, if necessary, or at least enough spacer cross-links are added to substantially cover the channels. The spacer cross-links may be attached by screws, spring loaded clamps, or other locking components. Once all of the determined attachment cross-links and spacer cross-links are added to the plate, the device is fully assembled and the surgical site may be closed.

Referring now in detail to the drawing figures, wherein like reference numerals represent like parts throughout the several views, FIG. 1A illustrates an exemplary embodiment of a plate 110 of an anterior cervical instrumentation system 100. The plate 110 may be substantially flat, as shown, or curved, not shown, and may have a thickness ranging from 1-3 millimeters (mm). In an embodiment, the plate 110 may be 2 mm thick. The plate 110 may be rectangular in shape, having a proximal and distal end. The plate 110 may measure 12-120 mm in length and 14-18 mm in width. In an embodiment, the plate 110 may be approximately 18 mm long and approximately 16 mm wide. The edges and corners of the plate 110 may be square, or rounded or smoothed to reduce potential damage or trauma to surrounding bone and/or tissue when implanted.

The plate 110 is adapted to be implantable in the human body, for example, on the cervical portion of the spine. The plate 110 may be composed of a suitable biocompatible or sterilizable material such as stainless steel, titanium, titanium alloys, memory alloys, nitinol, amorphous metal alloys, plastic, ceramic compounds, polymer compounds, carbon fiber, or another suitable material. The plate may be texturized, treated or coated on a portion or all of one or more sides to aid in joining of component parts, for bone growth or enhancement, to provide antimicrobial function, or immune response control.

The plate 110 may comprise a first aperture 120 a and a second aperture 120 b, both disposed at the proximal end of the plate 110. The radius of the apertures 120 a and 120 b may be between 4-6 mm. In an embodiment, the radius of the apertures 120 a and 120 b may be approximately 4.6 mm. The radius of the apertures 120 a and 120 b may correspond to the diameter of bone screws that will be used to secure plate 110 to the bone at a target site. The distance between the centers of the aperture 120 a and 120 b may be between 6-12 mm. In an embodiment, the distance between the centers of the aperture 120 a and 120 b may be approximately 9 mm. The plate 110 may further comprise a third aperture 120 c and a fourth aperture 120 d disposed at the distal end of the plate 110. The dimensions and arrangement of the third and fourth apertures 120 c relative to the plate 110 may be substantially identical to the first and second apertures 120 a and 120 b.

The interior perimeters of the apertures 120 a-d may be substantially cylindrical. In such embodiments, the apertures 120 a-d are adapted to interface with a round head surgical screw or fastener. The head of such a fastener may extend above the surface of the plate 110 when threaded through one of the apertures 120 a-d. This may not be optimal in situations where a minimal profile of the plate 110 and system 100 is desired. In other embodiments, at least a portion of the interior perimeter of the apertures 120 a-d may be frusto-conical. In such embodiments, the apertures 120 a-d may be adapted to interface and receive the angled surface of a flat head surgical screw or fastener. The head of such a fastener would be flush with the surface of the plate 110 when threaded though one of the apertures 120 a-d.

In exemplary embodiments of the plate 110, the interior perimeter of the apertures 120 a-d may be substantially smooth. The apertures 120 a-d may be substantially wide enough to enable the entire width of the fastener, including the treads, to pass through. In such embodiments, the plate 110 would be secured to the surface of the bone at least partial due to the compression caused by tightening the screw or fastener. In other contemplated embodiments, the interior perimeter of the aperture 120 a-d may be counter-threaded to correspond to the threading on a selected screw or fastener. In such embodiments, the fastener may be threaded through apertures 120 a-d and engage the bone to provide a secure attachment of the plate 110 to the vertebrae.

The plate 110 may further comprise a first channel 130 a and a second channel 130 b. The first and second channels 130 a and 130 b span the thickness of the plate 110 to provide elongated openings in the plate. The first and second channels 130 a and 130 b are elongate and extend in the distal-proximal direction. The first channel 130 a may be disposed between and axially aligned with the first and third apertures 120 a and 120 c. Similarly, the second channel 130 b may be disposed between and axially aligned with the second and fourth apertures 120 b and 120 d.

The channels 130 a and 130 b may be adapted to receive a fastener substantially similar to the fasteners used to secure plate 110 to the vertebrae through apertures 120 a-d as described above. The width of the channels 130 a and 130 b may be substantially equal to the width of apertures 120 a-d. The length of the channels 130 a and 130 b may be between 14-100 mm. In an embodiment, the length of the channels 130 a and 130 b may be approximately 20 mm. The channels 130 a and 130 b may be centered between apertures 120 a-d such that the ends of the channels 130 a and 130 b are equidistant from the nearest aperture 120 a-d.

The interior perimeter of the channels 130 a-130 b may be substantially smooth. This may enable the body of a fastener passing through the channels 130 a-130 b to smoothly translate in the distal to proximal direction. This feature allows for the attachment cross-links elements, described below, to “float” relative to the plate 110.

The plate 110 may be adapted to attach to vertebrae using temporary pins, surgical screws or fasteners as described above as attachment elements. In particular, the plate 110 is adapted to be disposed on the anterior side of the cervical portion of the spinal column. In other contemplated embodiments, the plate 110 may by used in other regions of the spinal column or other bones of the body.

FIG. 1B shows exemplary plates wherein the distal and proximal end apertures 120 e-h are elongated, or wherein the proximal apertures 120 i,j are elongated and the distal apertures 120 k,l are round. For elongated apertures, the vertical length of the aperture may be 6-8 mm. The apertures and channels 130 c,d may be as described in FIG. 1A.

FIG. 1C shows an exemplary plate wherein the channels 130 g and 130 h are located substantially from near the proximal end of the plate 110 to near the distal end of the plate 110, and provide an opening from the anterior to the posterior sides of the plate 110. There are no end apertures. A central midline aperture 120 m is shown as an elongated aperture, but may be a round or other shaped aperture (not shown). The plate, aperture and channels may be as described for FIGS. 1A and 1B.

FIG. 1D illustrates a side view of an exemplary embodiment of a plate 110 attached to a region of the spinal column. The plate 110 may be attached to a first vertebra 150 a by means of fasteners threaded through the first and second apertures 120 a and 120 b and engaging the bone. Because the depiction is a side view, it is difficult to distinguish in the illustration between the first and second apertures as one is directly behind the other. Further, the channels 130 a and 130 b are not depicted in the drawing.

The plate 110 may be positioned such that the proximal end is directly above the first vertebra 150 a. The surgeon may maneuver the plate 110 such that the first and second apertures 120 a and 120 b are directly over a target drill site, or a site for placement of a dual-headed pin, or two pins. The surgeon may mark the drill sites, remove the plate 110, and use a guide to drill holes of the appropriate depth at the target drill sites. Alternatively, the surgeon may leave the plate in place and either use the plate as a drill guide or place a drill guide atop the plate to drill the necessary holes. Alternatively, the surgeon may leave the plate in place and provide a dual-headed pin through both apertures 120 a and 120 b simultaneously. A dual-headed pin or two pins may be placed through apertures 120 c and 120 d. One of the dual-headed pins is then removed, and the surgeon may then attach the plate 110 to the first vertebra using the selected screw or fastener. The other dual-headed pin or two pins are removed, and screws are placed through the plate apertures and into the bone.

The above process may be substantially repeated to attach the distal end of the plate 110 to a second vertebra 150 b. This will lock the first and second vertebrae 150 a and 150 b in position relative to each other. The first and second vertebrae 150 a and 150 b are preferably on opposite sides of a target vertebra 150 c or vertebrae undergoing treatment. The vertebra 150 c undergoing treatment may be attached to the plate 110 using cross-linking elements, as will be described below.

Given the differences in anatomy and injuries between patients, and number of vertebrae undergoing treatment, the distance between suitable attachment sites on the first and second vertebrae may differ substantially from the distance between the first and second apertures 120 a and 120 b at the proximal end of the plate 110 and the third and fourth apertures 120 c and 120 d at the distal end. To enable optimal fitment, the system 100 may comprise a plurality of plates of variable lengths.

FIG. 2 illustrates an exemplary embodiment of a system having a plurality of plates. In this exemplary embodiment, the system 200 may comprise a first plate 210 a, a second plate 210 b, and a third plate 210 c. The plates 210 a-c may be substantially identical in design and dimension to plate 110 with the exception of the overall length of the plates and the elongate channels. Alternatively, a system may comprise plates of differing lengths as shown in FIG. 2, but plates in each size may have differently shaped apertures, or a central aperture, and/or channels are exemplified in FIGS. 1A-C.

The plates 210 a-c each may have a different length. In one embodiment, the difference between the lengths of the plates may be in an increment substantially equal to the height of a vertebra. In such an embodiment, the first plate 210 a could be intended to attach to a first and second vertebra, as described above, which have three target vertebrae undergoing treatment located there between. The second plate 210 b could be adapted to be used when two vertebrae are undergoing treatment. Similarly, the length of the third plate 210 c could make it suitable for situations where a single vertebra is undergoing treatment.

In other embodiments, the difference in length between the plates 210 a-c may correspond to the difference in lengths between desirable drilling sites on the vertebra of patients. For example, plates 210 a-c could be similar in length and adapted for use in situations where a single vertebra is undergoing treatment. The differences in the length of plates 210 a-c could correspond to the difference in the size of vertebra of patients. This would enable a surgeon to intraoperatively select the appropriate length plate to attach to the vertebra of a patient.

In other contemplated embodiments, the plates 210 a-c could have a wide range of lengths accounting for both applications with one or more target vertebra and vertebra of different sizes. In such embodiments, the system 200 may comprise more plates that the three illustrated. For example, the plates may incrementally vary in length to span an operational range from the shortest to the longest plate that may feasibly be used.

FIG. 3A illustrates embodiments of cross-linking elements. The cross-linking element 340 may be constructed from the same material as the plate 110 described above. The cross-linking element 340 may be substantially equal in length to the width of plate 110. The width of the cross-linking element 340 may be between 14-18 mm. In an embodiment, the cross-linking element may be 16 mm wide. The thickness of the cross-linking element 340 may be between 1-3 mm. In an embodiment, the cross-link may be 2 mm thick.

The cross-linking element 340 may comprise a first aperture 341 a and a second aperture 341 b. The dimensions and distance between apertures 341 a and 341 b may be substantially similar to those of apertures 120 a and 120 b.

The interior perimeters of the apertures 341 a and 341 b may be substantially cylindrical. In such embodiments, the apertures 341 a and 341 b are adapted to interface with a round head surgical screw or fastener. In other embodiments, a portion of the interior perimeter of the apertures 341 a and 341 b may be frusto-conical. In such embodiments, the apertures 341 a and 341 b may be adapted to interface and receive the angled surface of a flat head surgical screw or fastener.

In exemplary embodiments of cross-linking element 340, the interior perimeter of the apertures 341 a and 341 b may be substantially smooth. The apertures 120 a-d may be substantially wide enough to enable the entire width of the fastener, including the threads, to pass through. In other contemplated embodiments, the interior perimeter of the aperture 341 a and 341 b may be counter-threaded to correspond to the treads on a selected screw or fastener.

The cross-linking element 360 may be constructed from the same material as the plate 110 described above. The cross-linking element 360 may be substantially equal in length to the width of plate 110. The width of the cross-linking element 360 may be between 14-18 mm. In an embodiment, the cross-linking element may be 16 mm wide. The thickness of the cross-linking element 360 may be between 1-3 mm. In an embodiment, the cross-linking element may be 2 mm thick.

The cross-linking element 360 may comprise a first aperture 361 a and a second aperture 361 b. The dimensions and distance between apertures 361 a and 361 b may be substantially similar to those of apertures 120 a and 120 b.

The cross-linking element 370 may be constructed from the same material as the plate 110 described above. The cross-linking element 370 may be substantially equal in length to the width of plate 110. The width of the cross-linking element 370 may be between 14-18 mm. In an embodiment, the cross-linking element may be 16 mm wide. The thickness of the cross-linking element 370 may be between 1-3 mm. In an embodiment, the cross-linking element may be 2 mm thick.

The cross-linking element 370 may comprise a first aperture 371 a and a second aperture 371 b. The dimensions and distance between apertures 371 a and 371 b may be substantially similar to those of apertures 120 a and 120 b.

FIG. 3B shows an exemplary dual-headed pin 350. The pin has two pin heads 351 and 352, and a handle 353. The pin heads may be from 12-20 mm and a system may comprise one or more dual-headed pins having at least one of each of the 12-20 mm lengths. The handle 353 may be of any length that is suitable for holding or tapping by the surgeon.

FIG. 4A illustrates a top view of a plate and cross-linking elements of an exemplary embodiment of the system. In an exemplary embodiment, the system 400 may comprise a plate 410 having apertures 420 a-d, and cross-links. The plate 410 and cross-linking elements may be substantially similar to the plates and cross-linking elements described above. Cross-linking elements may be employed either as a spacer cross-link or as an attachment cross-link. In an embodiment, the system 400 comprises attachment cross-link 440 and 470, a first spacer cross-link 450, and a second spacer cross-link 460.

The attachment cross-link 440 may be coupled to the plate 410 by threading fasteners through apertures 441 a and 441 b and channels 430 a and 430 b, and engaging the vertebra disposed below the plate. In an embodiment, the attachment cross-link 440 is not fixed in position relative to plate 410. Rather, attachment cross-link 440 may move atop the plate 410 as the fasteners glide though channels 430 a and 430 b.

The attachment cross-link 470 may be coupled to the plate 410 by threading fasteners through apertures 471 a and 471 b and channels 430 a and 430 b, and engaging the vertebra disposed below the plate. In an embodiment, the attachment cross-link 470 is not fixed in position relative to plate 410. Rather, attachment cross-link 470 may move atop the plate 410 as the fasteners glide though channels 430 a and 430 b.

Spacer cross-links 450 and 460 may be disposed on both sides of the attachment cross-link 440 and proximal to cross-link 470 to limit their degrees of motion. In an exemplary embodiment, the first spacer cross-link 450 may be attached to the plate 410 on the proximal side of the attachment cross-link 440. The second spacer cross-link 460 may be attached on the distal side of the attachment cross-link 440, and proximal to attachment cross-link 470. The spacer cross-links 450 and 460 may be attached to the plate 410 using a fastener, such as a hole to hole clamp, a screw head, or short screw, by means of channels 430 a and 430 b and apertures 451 a, 451 b, 461 a, and 461 b. The spacer cross-links 450 and 460 may be fixed in position relative to the plate 410 upon attachment to the plate. In other contemplated embodiments, the spacer cross-links 450 and 460 may be spring loaded or employ spring loaded fastening elements to attach to the plate 410. There are multiple different spring loaded fastening elements known in the art and the decision for which fastening elements to use is within the knowledge of those skilled in the art.

The attachment position of spacer cross-links 450 and 460 may be selected to limit the range of motion of the attachment cross-links 440 and 470 as desired. The cross-links minimize rotational movement. Upon coupling to the plate 410, spacer cross-links 450 and 460 define how far attachment cross-links 440 and 470 may move along the plate 410 on channels 430 a and 430 b, as illustrated by the dashed arrows.

FIG. 4B illustrates a top view of a plate and cross-linking elements of an exemplary embodiment of the system. In an exemplary embodiment, the system 410 may comprise a plate 410 having only a central aperture 420 e, two channels that are located from an area near the proximal end to an area near the distal end, and cross-linking elements. The plate 410 and cross-linking elements may be substantially similar to the plates and cross-linking elements described above. Cross-linking elements may be employed either as a spacer cross-link or as an attachment cross-link. In an embodiment, the system 410 comprises attachment cross-links 445, 475 and 490, and spacer cross-links 455, 465 and 480.

The attachment cross-links 445, 475 and 490 may be coupled to the plate 410 by threading fasteners through apertures 446 a and 446 b, 476 a and 476 b, 491 a and 491 b, respectively, and through channels 435 a and 435 b, and engaging the vertebrae disposed below the plate. In an embodiment, the attachment cross-links 445, 475 and 490 are not fixed in position relative to plate 410. Rather, attachment cross-link 445, 475 and 490 may move atop the plate 410 as the fasteners glide though channels 435 a and 435 b.

Spacer cross-links 455, 465 and 480 may be disposed on the plate 410 to limit the degrees of motion of attachment cross-links 445, 475 and 490. In an exemplary embodiment, spacer cross-link 455 may be attached to the plate 410 on the proximal side of the attachment cross-link 445. Spacer cross-link 465 may be attached on the distal side of the attachment cross-link 445, and proximal to attachment cross-link 475. Spacer cross-link 480 may be attached on the proximal side of the attachment cross-link 490. The spacer cross-links 455, 465 and 480 may be attached to the plate 410 using a fastener, such as a hole to hole clamp, a screw head, or short screw by means of channels 435 a and 435 b and apertures 456 a, 456 b, 466 a, and 466 b, 481 a and 481 b, respectively. The spacer cross-links 455, 465 and 480 may be fixed in position relative to the plate 410 upon attachment to the plate. In other contemplated embodiments, the spacer cross-links 455, 465 and 480 may be spring loaded or employ spring loaded fastening elements to attach to the plate 410. There are multiple different spring loaded fastening elements known in the art and the decision for which fastening elements to use is within the knowledge of those skilled in the art.

The attachment position of spacer cross-links 455, 465 and 480 may be selected to limit the range of motion of the attachment cross-links 445, 475 and 490 as desired. The cross-links minimize rotational movement. Upon coupling to the plate 410, spacer cross-links 455, 465 and 480 define how far attachment cross-links 445, 475 and 490 may move along the plate 410 on channels 430 a and 430 b, as illustrated by the dashed arrows. The attachment cross-links are also limited in movement by the ends of the channels 435 a and 435 b.

In other contemplated embodiments, multiple attachment cross-links could be used with a multiple spacer cross-links. For example, a spacer cross-link could be attached to the middle of the plate and attachment cross-links placed on either side. The ends of the channels 435 a and 435 b and the spacer cross-link would limit the range of motion of the attachment cross-links. In other embodiments, various configurations and spacer and attachment cross-links are contemplated to attain a desirable result for a particular application.

FIG. 5 illustrates a side view of an exemplary embodiment of the device 500 and system attached to a spinal column. Plate 510 may be attached to a first vertebra 550 a and a second vertebra 550 b in substantially the same manner as plate 110 described above, using fasteners through apertures 520 a-d. The attachment cross-link 540 may be placed atop plate 510 and attached to the a target vertebra 550 c by passing a fastener 580 through the apertures of the cross-link 540 and channels (not pictured) of the plate 510 and engaging with a hole in the vertebra 550 c.

Spacer cross-links 550 and 560 may be attached to the plate in a fixed position as described above. The attachment cross-link 540 may move along plate 510 as the fasteners glide through the channels of the plate 510. The movement of the attachment cross-link 540 is limited by the spacer cross-links 550 and 560. Attachment cross-link 540 may move upward until it comes in contact with the first spacer cross-link 550. Similarly, attachment cross-link 540 may move downward until it comes in contact with the second spacer cross-link 560.

Movement of attachment cross-link 540 enables the target vertebra 550 c to move up and down, relative to the first and second vertebrae 550 a and 550 b. This movement or subsidence allows for bone-to-bone contact.

Another aspect of the present invention comprises devices and systems for adapting interbody spacers or cages to the plating systems of the present invention. There are several interbody spacers or cages currently available, such as those depicted in FIGS. 6A-D. These systems include an interbody spacer that fits within a disc space and is attached to the adjacent vertebral bodies by attachment elements or fasteners, such as a screws or other metallic fixation elements.

For example, Globus has introduced an interbody spacer known as the COALITION™ system, which is shown in FIG. 6A. The Globus system comprises an interbody spacer 600 having a textured surface 605 that contacts adjacent vertebral bodies, which aids in the attachment or stability of the interbody spacer 600. Such a surface may be referred to as a torsion stabilizer. The interbody spacer 600 can have various dimensions so as to conform to the appropriate anatomical size and features of the subject. For example, the interbody spacer 600 can have a width of about 14 mm and a depth of about 12 mm, a width of about 16 mm and a depth of about 14 mm, or a width of about 18 mm and a depth of about 15 mm. These interbody spacers can have a depth ranging from about 6 mm to about 12 mm. The interbody spacer 600 comprises two screws 610 a and 610 b, which attach the interbody spacer 600 to adjacent vertebral bodies. In the Globus system, the screws 610 comprise a head 612, a threaded shank 613, and a hexagonal socket 615. Generally, the screws 610 a-b are variable angle or fixed angle screws and have a length of about 3.6 mm or about 4.2 mm. The interbody spacer 600 further comprises a locking mechanism 620 that locks the screws 610 a-b in place, thereby inhibiting the screws 610 a-b from backing out of their fixed position. FIG. 6B illustrates a cross-sectional view of the Globus system interbody spacer 600 attached to adjacent vertebral bodies 625.

In another example, Synthes has introduced an interbody spacer known as the Zero-P system, which is shown in FIG. 6C. The Synthes system comprises an interbody spacer 600 having a textured surface 605 that contacts adjacent vertebral bodies, which aids in the attachment or stability of the interbody spacer 600. The Synthes interbody spacer 600 comprises four screws 610 a-d, which attach the interbody spacer 600 to adjacent vertebral bodies. In the Synthes system, the screws 610 a-d comprise a head 611, a threaded shank 612, and a hexagonal socket 615. When affixed to the interbody spacer 600, the screws 610 a-d have a cranial/caudal angle of about 40°±5° and a medial/lateral angle of about 2.5°. FIG. 6D illustrates a cross-sectional view of the Synthes system interbody spacer 600 attached to adjacent vertebral bodies 625.

The spacers described above can have lordosis ranging from about 0 degree of lordosis to about 7 degrees of lordosis. As used herein, “lordosis” refers to the sagital profile of an interbody spacer. For example, a spacer having parallel ends demonstrate 0 degree of lordosis, whereas a spacer having non-parallel ends exhibit exhibits greater than 0 degree of lordosis, such as 7 degrees of angulation front to back.

As evidenced in these two examples, multiple companies are manufacturing interbody spacer devices. They are designed to theoretically provide the strength of a standard anterior cervical discectomy and fusion procedure (ACDFP) with minimal disruption of the adjacent anatomy and with a minimal profile. However, none of the systems currently available has a system or a supplemental system for support when adjacent level disease occurs in adjacent vertebrae and requires surgery.

An embodiment of the present invention comprises a cross-linking element adapted to connect an interbody spacer 600 to a plate 110. FIGS. 7A-B illustrates embodiments of an adapting cross-link. The adapting cross-link 700 may be constructed from the same material as the plate 110 described above. The adapting cross-link 700 may be substantially equal in length to the width of plate 110. The adapting cross-link 700 may be substantially equal in length to the width of interbody spacer 600. Thus, the width of the adapting cross-link 700 may be between about 14 to about 18 mm. The thickness of the adapting cross-link 700 may be between about 1 to about 3 mm.

As shown in FIG. 7A, the adapting cross-link 700 may comprise a first aperture 705 a and a second aperture 705 b. The dimensions and distance between apertures 705 a and 705 b may be substantially similar to distance between the screws 610 a and 610 b of the interbody spacer shown in FIG. 6A. In another embodiment, the adapting cross-link 700 may comprise a first aperture 705 a, a second aperture 705 b, a third aperture 705 c, and a fourth aperture 705 d, as shown in FIG. 7B. The dimensions and distance between apertures 705 a-d may be substantially similar to distance between the screws 610 a-d of the interbody spacer 600 shown in FIG. 6C. Of course, one of ordinary skill in the art could readily design an adapting cross-link 700 having apertures that substantially conform to the location and/or number of attachment elements for a given interbody spacer system. In addition, a plate 110 and its apertures and channels can be designed to accommodate or substantially conform to the location and/or number of attachment elements for a given interbody spacer system. Thus, for example, a plate designed to support an interbody spacer having two attachment elements may have two channels, and a plate designed to support an interbody spacer having four attachment elements may have four channels.

In an embodiment of the present invention, a coupling element 800, which is shown in FIGS. 8A-B, is used to attach the adapting cross-link 700 to the interbody spacer 600. The coupling element 800 may comprise many fasteners, such as pins, dual head pins, or screws, among others. In another embodiment, the coupling element 800 can operate to attach not only the adapting cross-link 700 to the interbody spacer 600 but also to attach the interbody spacer 600 to a vertebra.

In one exemplary embodiment, the coupling element 800 is configured to engage the socket 615 of the head 611 of a screw 610 for an interbody spacer 600. (FIGS. 9A-B) The coupling element 800 comprises: an elongated member 805 that is adapted to mate with the socket 615 of the interbody spacer screw 610, a shank 810 that is adapted to substantially traverse the adapting cross-link 700, and a cap 815 configured to attach the coupling element 800 to the adapting cross-link 700. In an exemplary embodiment, the coupling element 800 comprises an hexagonal elongated member 805, a threaded shank 810, and a locking cap 815. The coupling element 800 and it associated components or sections can be made of the same or different materials, such as steel, titanium, plastics, ceramics, or other biocompatible materials.

Considering that the coupling element 800 is configured to engage and mate with the socket 615 of the head 611 of a screw 610 for an interbody spacer 600, the elongated member is designed to accommodate the angle of entry of the screw for the interbody spacer. This accommodation can be accomplished in one of two ways: configuring the elongated member 805 to adopt the angle of entry of the screw 610 for the interbody spacer or inserting the coupling member 800 in the adapting cross-link 700 at angle that is substantially similar to the angle of entry of the screw 610 for the interbody spacer. Therefore, the elongated member may project substantially parallel to the longitudinal angle of the fastener of the interbody spacer. In some embodiments, however, the elongated member may project substantially non-parallel to the longitudinal angle of the fastener of the interbody spacer.

In one embodiment, the elongated member 805 can project from the shank 810 of the coupling element 800 at substantially the same angle as the screw 610 for interbody spacer (FIG. 8A). In such an embodiment, the shank 810 of the coupling element 800 is inserted through the adapting cross-link 700 substantially perpendicular to the mounting surface of the interbody spacer 600. (FIG. 9A) Alternatively, the elongated member 805 can project substantially parallel to the longitudinal axis of the shank 810 of the coupling element 800. (FIG. 8B). In such an embodiment, the shank 810 of the coupling element 800 is inserted through the adapting cross-link 700 at substantially the same angle as the screw 610 for interbody spacer 600. (FIG. 9B) Considering that the elongated member 805 is configured to engage and mate with the socket 615 of the screw 610 for the interbody spacer 600, a person of skill in the art would realize that the shape and size of the elongated member 805 can vary based upon the shape and size of the socket 615 of the screw 610. For example, the elongated member 805 can have many shapes, including but not limited to, an hexagonal shape, a star shape, a cross shape, and a square shape.

Given the various configurations of the elongated member 805, an aperture 705 of the adapting cross-link 700 may define a channel 905 that is substantially perpendicular to the mounting surface of the interbody spacer 600 or an aperture 705 may define a channel 910 that has substantially the same angle as the screw for interbody spacer.

The interior perimeters of the apertures 705 may be substantially cylindrical. In such embodiments, the apertures 705 are adapted to interface with a round coupling element 800. In other embodiments, a portion of the interior perimeter of the apertures 705 may be frusto-conical. In such embodiments, the apertures 705 may be adapted to interface and receive the angled surface of a frusto-conical coupling element 800.

In exemplary embodiments of an adapting cross-link 700, the interior perimeter of the apertures 705 may be substantially smooth. The apertures 705 may be substantially wide enough to enable the entire width of the coupling element 800, including the threads, to pass through. In other contemplated embodiments, the interior perimeter of the aperture 705 may be counter-threaded to correspond to the threads on the coupling element 800.

In one embodiment, the coupling element 800 is modular and comprises three distinct components: the elongated member 805, the threaded shank 810, and a locking cap 815. In such an embodiment, the coupling element 800 can be threaded through the adapting cross-link 700, the elongated member 805 would engage and mate with the socket 615 of the screw 610 for the interbody spacer 600, and the locking cap 815 would be positioned to lock the coupling element 800 in place, effectively attaching the adapting cross-link 700 to the interbody spacer 600.

The adapting cross-link 700 can also operate as an attachment cross-link or a spacer cross-link. Accordingly, the adapting crosslink 700 may have features similar to those described above for attachment cross-links or a spacer cross-links.

Although not wishing to be bound by any particular theory, an adapting cross-link 700 can be used to couple a plate 110 to an interbody spacer 600 in the event that adjacent level disease occurs in vertebrae adjacent to the location of the interbody spacer 600. According to the various embodiments of the present invention, the plate 110 may be coupled to a interbody spacer 600 before or after implantation of the interbody spacer 600. To this end, the plate 100 may be an integrated component 110 of the interbody spacer 600 (e.g., it may be manufactured as part of the interbody spacer) or it may be used to supplement a pre-existing interbody spacer 600. If adjacent levels are treated by coupling a plate 110 to an interbody spacer 600, the flexible insertion points of the above described plates 110 and associated attachment and spacer cross-links would allow the involved adjacent vertebral bodies to be reinforced by placement of the plate attached to the vertebral bodies.

The modular nature of the plating system and the ability to position cross-links of various types at exact positions along the plate allow the plate to be used in multiple configurations with the interbody spacer systems. For example, the devices and systems of the present invention can be used to reinforce interbody spacers when more than one level is treated. (See FIGS. 10-12). The devices and systems of the present invention can allow for different types of interbody spacers to be reinforced at an initial surgery or at a subsequent surgery. One example of this would be the treatment of adjacent vertebral levels. The plating system of the present invention provides additional support if a second or third level were to be surgically approached. This would not be limited to just interbody spacers, as the flexibility the plates 110 described herein would allow for various constructs to be reinforced, including but not limited to; two adjacent interbody spacers 600 of the same type or of intermixed systems (FIG. 10A), interbody spacers 600 separated by a non treated level 627 (i.e., non-adjacent spacers) (FIG. 10B), interbody spacers 600 adjacent to standard ACDF 601 (FIG. 10C), which can be reinforced with an attachment cross-link 440 and a plurality of fasteners 613.

FIG. 11 provides a front view of a plate coupled to three interbody spacers, demonstrating that the plate allows for reinforcement of multiple levels sequentially treated with interbody spacers. In an exemplary embodiment, the system comprises a plate 110 having only a central aperture 420 e, two channels that are located from an area near the proximal end to an area near the distal end, and cross-linking elements. The plate 110 and cross-linking elements may be substantially similar to the plates and cross-linking elements described above. Cross-linking elements may be employed as a spacer cross-link, an attachment cross-link, or an adapting cross-link. In this embodiment, the system comprises adapting cross-links 710, 720, and 730, and spacer cross-links 455, 465, and 480. This embodiment utilizes the Globus Interbody Spacers but other embodiments could be employed with other systems and with intermixed systems. The plate would allow reinforcement of multiple levels sequentially treated with interbody spacers,

The adapting cross-links 710, 720, and 730 can be coupled to the plate 110 by threading coupling elements 800 through apertures 711 a and 711 b, 721 a and 721 b, 731 a and 731 b, respectively, and through channels 435 a and 435 b, and engaging the screws of the interbody spacer disposed below the plate. In an embodiment, the adapting cross-links 710, 720, and 730 are not fixed in position relative to plate 110. Rather, adapting cross-link 710, 720, and 730 may move atop the plate 110 as the coupling elements 800 glide though channels 435 a and 435 b.

Spacer cross-links 455, 465 and 480 may be disposed on the plate 110 to limit the degrees of motion of adapting cross-links 710, 720, and 730. The spacer cross-links 455, 465 and 480 may be attached to the plate 110 using a fastener, such as a hole to hole clamp, a screw head, or short screw by means of channels 435 a and 435 b and apertures 456 a, 456 b, 466 a, and 466 b, 481 a and 481 b, respectively. The spacer cross-links 455, 465 and 480 may be fixed in position relative to the plate 110 upon attachment to the plate. In other contemplated embodiments, the spacer cross-links 455, 465 and 480 may be spring loaded or employ spring loaded fastening elements to attach to the plate 110. There are multiple different spring loaded fastening elements known in the art and the decision for which fastening elements to use is within the knowledge of those skilled in the art.

The attachment position of spacer cross-links 455, 465 and 480 may be selected to limit the range of motion of the adapting cross-links 710, 720, and 730, as desired. The cross-links minimize rotational movement. Upon coupling to the plate 110, spacer cross-links 455, 465 and 480 define how far adapting cross-links 710, 720, and 730 may move along the plate 110 on channels 430 a and 430 b, as illustrated by the dashed arrows. The adapting cross-links are also limited in movement by the ends of the channels 435 a and 435 b.

In other contemplated embodiments, multiple adapting cross-links could be used with multiple spacer cross-links and/or multiple attachment cross-links to attain a desirable result for a particular application.

The plating devices and systems of the present invention also allow for the salvage of an interbody spacer that was not progressing satisfactorily. For example, a plate could be used to provide additional support at the level treated. The removal of the screws of an interbody spacer can be done relatively simply, but removal of the spacer itself would be much more difficult. The various embodiments of the present invention would allow the interbody spacer 600 to be reinforced with (FIG. 12A) or without (FIG. 12B) the removal of the screws 610 a and 610 b used in the interbody spacer 600 while allowing the interbody spacer 600 to remain within the disc space. In using a plate to reinforce an interbody spacer, the plate can be installed at the same time as the interbody spacer or subsequently as a salvage procedure.

In another embodiment of the present invention, a plating system can be attached to an interbody spacer by way of the locking mechanism of the interbody spacer. FIG. 13 illustrates an exploded side view of such an embodiment. Many interbody spacers that are currently available incorporate some type of locking mechanism, such as a locking cap 620. An embodiment of the present invention comprises a coupling element 850 that is capable to attach a plate 110 to an interbody spacer 600. The coupling element 850 comprises an interfacing element 851 and a connecting element 853.

The interfacing element 851 of the coupling element 850 is adapted to matingly engage a locking cap 620. In some embodiments, interfacing element 851 of the coupling element 850 is adapted to matingly engage a locking cap 620 and to contact at least a portion of the anterior surface of an interbody spacer 600. Thus, it is an object of the present invention to configure the coupling element 850 so that it can matingly engage any interbody spacer, effectively producing a global adapter to couple any interbody spacer to the plating systems of the present invention.

In some interbody spacers, the locking mechanism 620 is flush with the anterior surface of the interbody spacer 600. In such embodiments, the coupling element 850 comprises corresponding raised elements to engage the locking mechanism. In other embodiments, the locking mechanism 620 may slightly protrude or project from the anterior surface of an interbody spacer 600. In such an embodiment, the coupling element 850 can be capable of receiving a portion of the locking mechanism 620.

The connecting element 853 of the coupling element 850 is adapted to connect the interbody spacer to a plate 110. To this end, the connecting element 853 of coupling element 850 is configured to traverse a channel or aperature of the plate 110 and engage an adapting cross-link 700. The coupling element 850 can be configured to traverse one or more channels or aperatures of the plate 110 and engage an adapting cross-link 700. The adapting cross-link can be coupled to the coupling element 850 through a fastener, such as a screw 860. In one embodiment, an adapting crosslink can be compressed with a screw 860 onto the plate 110 and the coupling element 850, which in turn compresses the coupling element 850 onto the locking cap 620, effectively connecting the interbody spacer 600 to the plate 110.

The various embodiments described above are intended to enable a surgeon to intraoperatively customize the anterior cervical instrumentation system for optimal application. Consequently, the embodiments described above are merely exemplary and not limiting. In particular, the configurations, dimensions and orientation of components described above may be modified from what has been recited and described without departing from the design of the invention. Further, embodiments of the present invention are not limited to applications in the anterior region of the spine. Particularly, the embodiments of the present invention can also be used in the thoracic and lumbar regions. 

1. A vertebral stabilization system comprising: an interbody spacer device configured to be installed in an intervertebral space with a first fastener and a second fastener; an elongate, rectangular plate, the plate having an anterior side, a posterior side, a distal end, and a proximal end, the plate further comprising a first elongate channel and a second elongate channel, the first and second channels being substantially parallel, substantially equal in length, and extending along the plate between the distal end and the proximal end, wherein the posterior side of the plate is disposed on the interbody spacer so that the first channel is substantially aligned with the first fastener and the second channel is substantially aligned with the second fastener; a first adapting cross-link having an elongate rectangular body having a first aperture and a second aperture, the first and second apertures substantially aligned with the first and second channels when the first adapting cross-link is disposed on the anterior side of the plate; and a coupling element configured to engage at least a portion of the interbody spacer device, wherein the first or second apertures receive the coupling element effective to attach the adapting cross-link to the interbody spacer through the plate.
 2. The vertebral stabilization system of claim 1, further comprising a first spacer cross-link having an elongate rectangular body having a third aperture and a fourth aperture, the third and fourth apertures aligned with the first and second channels when the first spacer cross-link is disposed on the anterior side of the plate.
 3. The vertebral stabilization system of claim 2, wherein the first adapting cross-link can move relative to the plate as the first and second coupling elements slide along the first and second channels.
 4. The vertebral stabilization system of claim 3, wherein the first spacer cross-link attached to the plate by third and forth fasteners passing through the third aperture and fourth apertures and engaging the first and second channels, respectively, wherein the first spacer cross-link does not move relative to the plate and limits movement of the first adapting cross-link relative to the plate.
 5. The vertebral stabilization system of claim 1, further comprising a first attachment cross-link having an elongate rectangular body, the first attachment cross-link having a fifth aperture and a sixth aperture, the fifth and sixth apertures aligned with the first and second channels when the first attachment cross-link is placed on the anterior side of the plate.
 6. The vertebral stabilization system of claim 1, wherein a coupling element comprises an interfacing element and a connecting element, wherein the interfacing element is adapted to matingly engage at least a portion of the interbody spacer and the connecting element is configured to traverse a channel or aperture of the plate and engage the adapting cross-link.
 7. The vertebral stabilization system of claim 1, wherein a coupling element comprises a cap, a an elongated member, and a shank extending between the elongated member and the cap, and wherein the elongated member is adapted to mate with at least a portion of the a fastener.
 8. The vertebral stabilization system of claim 7, wherein the elongated member projects substantially parallel to the longitudinal axis of the fastener of the interbody spacer.
 9. The vertebral stabilization system of claim 7, wherein the elongated member can projects from the shank at substantially the same angle as the fastener of the interbody spacer.
 10. A vertebral stabilization system comprising: a first interbody spacer device configured to be installed in a first intervertebral space with a first fastener and a second fastener; a second interbody spacer device configured to be installed in a second intervertebral space with a third fastener and a fourth fastener; an elongate, rectangular plate, the plate having an anterior side, a posterior side, a distal end, and a proximal end, the plate further comprising a first elongate channel and a second elongate channel, the first and second channels being substantially parallel, substantially equal in length, and extending along the plate between the distal end and the proximal end, wherein the posterior side of the plate is disposed on the first and second interbody spacers so that the first channel is substantially aligned with the first fastener of the first interbody spacer device and the third fastener of the second interbody spacer device and so that the second channel is substantially aligned with the second fastener of the first interbody spacer device and the fourth fastener of the second interbody spacer device; a first adapting cross-link having an elongate rectangular body having a first aperture and a second aperture, the first and second apertures substantially aligned with the first and second channels when the first adapting cross-link is disposed on the anterior side of the plate; and a first coupling element configured to engage at least a portion of the first interbody spacer device, wherein the first or second apertures receive the first coupling element effective to attach the first adapting cross-link to the first interbody spacer through the plate; a second adapting cross-link having an elongate rectangular body having a third aperture and a fourth aperture, the third and fourth apertures substantially aligned with the first and second channels when the second adapting cross-link is disposed on the anterior side of the plate; and a second coupling element configured to engage at least a portion of the second interbody spacer device, wherein the third or fourth apertures receive the second coupling element effective to attach the second adapting cross-link to the second interbody spacer through the plate. 